Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,988 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
1,988 in last 12 months

Showing 99619980 of 28,641 recalls

Medical DeviceMarch 22, 2021· Datascope Corp.

Recalled Item: Cardiosave Hybrid IABP - Product Usage: used to inflate and Recalled by...

The Issue: There are cybersecurity vulnerabilities in a widely used low-level TCP/IP...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP Recalled...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· Normand-Info S.A.S.U.

Recalled Item: Normand Remisol Advance Data Manager is a software device that Recalled by...

The Issue: Instructions For Use for software versions 1.5 to 1.9 did not provide...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) Recalled by BIOPSYBELL...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT SINGLE - ACCESS Recalled by BIOPSYBELL S.R.L. Due to Products...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica CEMIX Recalled by BIOPSYBELL S.R.L. Due to Products labeled as...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· QURA S.R.L.

Recalled Item: Spectrum Medical Quantum Standard heat exchanger Recalled by QURA S.R.L. Due...

The Issue: Product labeled as sterile may not have been adequately sterilized. In...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: EASYNJECT Recalled by BIOPSYBELL S.R.L. Due to Products labeled as sterile...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G COAXIAL CANNULA WITH TUOHY CONNECTION Recalled by BIOPSYBELL S.R.L. Due...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: CEMIX - CEMENT MIXING SYSTEM Recalled by BIOPSYBELL S.R.L. Due to Products...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10 GAUGE CEMENT DELIVERY CANNULA Recalled by BIOPSYBELL S.R.L. Due to...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT WORKING CANNULA DIAMOND TIP MINI Recalled by BIOPSYBELL S.R.L....

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT Recalled by...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G DIRECT SINGLE - ACCESS Recalled by BIOPSYBELL S.R.L. Due to Products...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing